meddevicedb.com FDA Device Reference

LAPAROTOMY PADS

K811769 Class I Traditional
Decision Date
1981-08-07
Sponsor / Applicant
South Mountain Medical

Technical Specification

510(k) Submission ID K811769
Product Code GDY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4450
Decision Date 1981-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAPAROTOMY PADS received FDA 510(k) clearance under submission number K811769, sponsored by South Mountain Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1981-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code GDY and 21 CFR 878.4450, within the General, Plastic Surgery review panel as a Class I device.